|Publication number||US2759869 A|
|Publication date||Aug 21, 1956|
|Filing date||Jan 5, 1952|
|Priority date||Jan 5, 1952|
|Publication number||US 2759869 A, US 2759869A, US-A-2759869, US2759869 A, US2759869A|
|Inventors||Martin M Reynolds, Melville G Sutton|
|Original Assignee||West Laboratories Inc|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (8), Referenced by (28), Classifications (14)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United, States Patent GERMICIDAL IQDINE PREPARATIONS- Melville G- utto r e 'Gard u Hi siNt taa drMantiu M. ReynoldgDrexel Hill, Pa., assignors to West Lab- Oratorics Inc LOng Island. City,,N'; Y., a corporation of New York N Drawing. Application January 5,1952,
Serial Not 265,192:
15 Claims. (Cl. 167- 70) The present invention is concerned with germicidal preparations of the: type efficacious in relatively dilute aqueous solutions.
As conducive to a clear understanding of. the inventign, it is noted that since iodine has but slight solubility in water (0.29 gram per liter), much of it will promptly precipitate upon dilution with Water from iodine solutions thereof in those commoniodine solvents that arerniscible With,water such as acetone, ethyl alcohol, methyl alcohol, glyqols and glycerols. Of course iodine will pass tonot more than the above mentioned extent; into, water. from solutionin water-immiscible solvents such as carbon tetrachloride, benzene and ether. Most anionic and cationic urfa nts. end o react with iod ne, re ulting: in: wa r insoluble products and. so here pr v o: b nerally unsatisfactory as iodine solvents,
It. is; among; the j cts. of. he; iny ut onl o provide: a germicidal pr parati n. f the. abov yp he: fo m: of IP- d I, on e r t or olu ion hat is-eeono niea rye horough y eflica i s, whi h ncorp r tes. as. 'tfir na-in germi id gent a large proportion, otelemeutal iodine hat is.v andremains; s ab lized toeac ants aeae ellul in aqueous: solutionof any dilution, and by the; action any microorganisms: to" which. the; preparation; is. applie d, is promgtly. r ndered effe iv but: subst n ial y alu ed-1e minute extent. necess ry for germicidal ctiom nd: sye
relatiyely O r Q or ly and'derma ologie llys.
Though. n i h rpolyp pylene xide. 3.0. nolue hyieue oxide regardless of. he: egre of ts vpolsgmer ae otn.wi l solubilize iodine inwater toiany marked.degree;. fliteinyautiou. is, based on. he surpri ng iscov ry hat ert in hemical comhiua ious; of, polun ouyl ne. and nolu thxleue oxidesmay be ren e ed servi eable. a unr c d edly xcellent! water sol bil z ge sie fo leme all odiue- More. u rticularln he. inv n n is b ed uoni he. discovery that such utility resides in a class; of, IlQllyiQIiiG surfactants characterized by. a hydrophobic group; consisting of propylene oxide polymerized to poly ogypropylene glycols and then reactedwith ethylene oxide,,which latter are polymerized to hydrophylic groups ofpoly; ethylene oxide-chains. V I
Qompositions of: thecharacter set forthare a-- product of Wyandotte Chemicals Corporation of Wyandotte, Michigan, and are designated by the term. "Pluronics-, a term; which; in the: interest; ofi brevity will be hereinafter sed: in; the specification to identify such. compositions. Th se. composi ions: have; been: d s los d! and claimed in S. Patent No. s datedzApril 6-,. L95 n d to Wyandotte Chemicals C rporation, a d definedl heneiu as compoundsaccon ing o: he fi rmula.
vaporizes in part, and the rest, far from enteringinto solution, combines chemically therewith to split the Ice Pluroni'c molecule, impairing its solubility in water and itsdetergent action. When, on the other hand, itis attempted to dissolve: large amounts of iodine insuch Rluronic at low temperature by resort to agitation for instance, notonly is the rate of solution too. slow for commercial utility, but' the resultantcloudiness generally occurring upon dilution intap water suggests precipitation: rather than solution.
If the iodine were once brought into solution in the Pluronic; it would be released by contact-- with microorganisms and would not be inordinately taken up by organic foreign matter such as proteins, milk solids, milk serums, peptone cultures, agar, gelatin and. the like that maybe presenti'n the medium to be germicidal'lytreated.
Anyalltali in such medium, would, howevergpombine very slowly witlrfree iodine from the Pluronic environment and to that extentrender the, iodine unavailable for germicidal action.
According to one feature of the-invention, the solution of a large proportion of; elemental iodine by a Plunonic is brought to pass under heat, without objectionable chemical action or any of the untoward eflects above noted, by the addition, of an acid such as hydrochloric acid, that is inert to iodine andthat acts to obviate the difiiculties previously pointed out, though in a manner nder ood y us Su h.v a moreover, combine with such organic foreign matter. Furthermore, it com bineslwith such alkali and thereby serves to protectthe o ine. from e ng, u e e ly pent. Bearing; in, mind hat only one part per. million, of iodinev (1 p p. n. is. required o ki l; mic oo ga sm the mpositi n. i hi iodine ontent husnro ecte ishi y economic l.-
In general, the acid used in dissolving iodine in liquid Pluronic shouldnotbe less thanZpercent andnot more than, 3' per cent and preferably about 2.5 per cent by weight. of, the. concentrate and. the solution of the-v iodine shouldbe effected in, the- Pluronic under agitationv at a temperatureot 45 C. to C.,.pr eferably about60- C.
For purposes of, definition, the term. Halophofl has been. coined and ishereafter used. to define a compound that, greatly increases, the solubility of; and tends, to stabilize iodine in, aqueous,systems to reactantsothenthan microorganisms.
Halophor Index? is defined and hereinafter used; to d ine heiodine. apa ity ofth .he p r hem aimum percentage, by; weight of iodine in. the resultant halophoniqdinee mnlexl ha w ll. giv a le rsol tiou n w er-at 224 C... to a y d lution. The y l odin rpree pitatr ice. rom th olution indi ates wh n,v the; halonhm n ex as b e exceeded- B uroniesaremade n a wi e var y o moles.- uler ght: f: the hydr pho g p, nd (-2) its e sh ratio. to. the hydrophylic gro p, whic eig nd; ra io are ont lolled. y he an fa rer: o p de eimine. he desired; characteristics, such, as. Wetting action, detergency, foam ng; p g y d hyg o c ni ity, m n her: physcalt ud chemic lt prz per es;
ngene ali od neant c o d h p s t nv a i ulbe dis olv d.- ui ny, Blut nie. A ma11. prop rtion o h i d ne ppears. ecom fixed as nio i l bu he major: PQ l Q l' e he od ne rem ns il le; as sucla apnarentln y: solution in the hydropho ic gro p and is; ilr tahle as; free, iodine. releasable. fro he: some position:as.theactivegermicides Determinations.- thus far made have indicated. t fii ot the Plunonios standardized by the manufac rer: and designated. Plupon-io I'd- 62- (a concentrate: essentially consisting of a definite predetermined; molecular Weight ofi the= hydrophobic group. with aldefinite, weight: ratio to the hydrophylic group) dissolves and maintainsdnistahle, aqueous solution when greatly diluted, a greater proportion of iodine than any other of the Pluronics tested or than any other solvent or composition heretofore known. In particular, Pluronic L-62 will dissolve 28 per cent by weight of iodine and thus has a halophor index of 28, and moreover has the further virtue of foaming but slightly. Pluronic L62 is therefore in generalprcferred for purposes of the present invention although the other standardized Pluronics now available are also satisfactory, since they dissolve large proportions of iodine, Pluronic L-64 for instance having a halophor index of 16, Pluronic 'L44 of 14, and Pluronic F-68, which is in solid or flaky form at room temperature, having a halophor index of 10. Pluronic L62 is a liquid condensate of polypropylene oxide and ethylene oxide, the polypropylene oxide group having a molecular weight Within the range of 1501 to 1800 and the condensate containing from 20 to 30 per cent by weight of ethylene oxide. Pluronic L-64 is a liquid condensate of polypropylene oxide and ethylene oxide, the polypropylene oxide group having a molecular weight within the range of 1501 to 1800 and the condensate containing from 40 to 50 per cent by weight of ethylene oxide. Pluronic L-44 is a liquid condensate of polypropylene oxide and ethylene oxide, the polypropylene oxide group having a molecular weight within the range of 1001 to 1200 and the condensate containing from 40 to 50 per cent by weight of ethylene oxide. Pluronic F68 is a condensate of polypropylene oxide and ethylene oxide in the form of flakes, the polypropylene oxide group having a molecular weight within the range of 1501 to 1800 and the condensate containing from 80 to 90 per cent by weight of ethylene oxide.
In commercial practice, the germicidal preparation of the present invention is to be marketed in bottles or drums in very dilute aqueous solution, for which purpose 5 to 25 per cent, preferably about to per cent, of lsopropyl-alcohol is included in the concentrate to assure easy and rapid dilution.
The use of distilled water as the diluent is economically unfeasible in most applications. While the use of soft tap water, and even of hard water, is feasible for the purpose, when the concentration of the composition as marketed considerably exceeds 1 per cent, resort to the preferred concentration to be marketed, of from .1 per cent to l per cent of the Pluronic-iodine complex in tap water, results in cloudiness, which renders the product unacceptable, even though such cloudiness does not detract from its efficacy as a germicide.
One of the characteristics of Pluronics is that under certain conditions of temperature and concentration in water, cloudy solutions result. The addition to such solution of a nonyl-phenol ethylene oxide that has preferably from about 8 to 9 mols of ethylene oxide per mol of nonyl-phenol which is sold by General Aniline & Film Corporation under the trade name Antarox A 400, results in a clarification of the solution over a wide range of temperatures. In other words the addition of such Antarox A400 to the composition greatly widens the range of dilution with ordinary tap water in which a clear solution is attained. For example, where a Pluronic iodine solution of a given concentration remains clear, say in the range of to 50 C., the addition of sufficient Antarox A-400 would both decrease the lower limit of such temperature and increase the upper limit, say to cover a range in which the solution remains clear, at from 10 to 65 C. Or, for any given temperature, the addition of the Antarox A-400 component substantially decreases the dilution (generally in the ratio of approxi mately 10:1), in which no cloudiness will occur.
The use of Antarox A-400 as an additive, attains yet another advantage, in that it improves the objectionable clouding of the composition induced by the addition of special ingredients, such for instance, as anaesthetics,
.illustratively the anaesthetic Cyoloform (isobutyl paraamino benzoate).
Anatrox A-400 is a single ring benzene compound with a polymer averaging eight ethylene oxide groups, each ethylene oxide group of the formula 0(CH2CH2O)H, attached in one position to the ring, and with iso-octyl or i-so-nonyl in the meta position on the ring.
According to another feature of the invention, solid, water soluble compositions inert to iodine under conditions of use and that serve as protective agents for the iodine may be added in order (1) greatly to extend the halophor index, (2) to reduce the cost of the product, and (3) to render possible the preparation of the ultimate Pluronic iodine composition in the form of a stable, dry powder, rather than a concentrate. For this purpose, it is desirable to use (in order of preference) sodium acid sulphate, solid organic acid, preferably citric acid or urea. To attain a dry product, the proportion of such added ureanitrate, sodium acid sulphate, citric acid or urea should be 70 per cent or more of the final product.
A few examples will now be given of germicidal compositions according to the invention, the parts being by weight.
Example I.Concentrate for cleaning sanitary equipment Parts Pluronic L-62 44 Hydrochloric acid (30% to 35%) .5 to 3 preferably 2 Iodine up to 17 Isopropyl alcohol (99%) 5 to 25 preferably 15 To this composition may be added 5 to 25 parts, preferably 20 parts, of Antarox A-400. The concentrate thus prepared has a density of about 1.12 and a cost of little more than 50 cents per pound. 72 fluid ounces of the concentrate when added to 100 gallons of tap water. goes into solution very readily and makes a commercially saleable product of 0.6 per cent of concentrate in water.
For making the concentrate, the Pluronic, acid and iodine ingredients are mixed in a stainless steel kettle and heated to from 45 C. to 75 C., preferably to about 60 C., while agitating the mass until all the iodine is in solution, the heating expediting the solution and helping to stabilize the final product. After the iodine is all in solution, the Antarox A-400 may be added and the mixture then cooled to about 40 C., whereupon the isopropyl alcohol is added, the solution becoming homogeneous after about five minutes of mild agitation.
The Antarox A-400 would be omitted if the solution were sold in concentrations considerably exceeding 1 per cent or if the cloudiness were not objectionable for any particular use. Antarox A-400 in amount less than above indicated, would be less efficacious in avoiding cloud formation.
With an acid content of less than .5 per cent, a reduced proportion of the iodine is available as germicide and if the acid content is above 3 percent the cloud point is adversely affected. Control of the acid content thus avoids impairing the stability or efi'iciency and clarity of the final product.
The concentrate described will titrate 13 percent plus or 750 p. p. m. of free iodine, which is available for its germicidal action. If maintained at about F. for more than three weeks, the iodine content will drop to about 500 stantially non-foaming.
Example lI';--F0l' topical application (firstaid, cuts, abrasions, etc.)
The iodine content should of course not exceed the halophor index.
The Pluronic, iodine and acid are mixed as inExample I to dissolve the iodine.
The cycloform and Antarox A-400 are dissolved in isopropyl alcohol.
The two mixtures thus prepared. are combined and maintained at 25 C. to 40 C., preferably at about 30 C., whereupon the distilled water is added.
One ounce of the solution to one cup of water provides an antiseptic wash.
One ounce of the solution to one quart of water provides a germicidal solution for sickroom utensils, feminine hygiene and the like.
Example III.-Rinse for dishes and kitchen utensils Parts Phosphoric acid (42%) 45 to 75 preferably 60 Pluronic L-62 25 to 45 preferably 3.5
Pluronic L-64 25 to 45 preferably 35 Iodine to 15 preferably Hydrochloric acid (cone) l to 4 preferably 2 Isopropyl alcohol 60 to 100 preferably 80 Water 600 to-900 preferably 780 With the use of the two dilferent Pluronics above indicated, the solution remains substantially clear under high dilution even in the absence of any Antarox A-400.
The phosphoric acid serves essentially as a protective agent for the iodine by neutralizing alkalis and alkaline salts.
To prepare the concentrate, the two Pluronics are mixed with the iodine and hydrochloric acid and warmed to between 40 C. to 70 C., preferably to about 50 C., until the iodine is in solution. Upon cooling to room temperature, the isopropyl alcohol and the phosphoric acid are mixed in. The concentrate is finally diluted by the addition of the water.
Example I V.Germicidal soap preferably 10 The Carbowax-6000 or polyethylene glycol of molecular weight of about 6000 solidifies the otherwise soft pro? duct, without detracting from the physical or chemical properties of the soap cake.
The flowers of sulphur serves to mask the otherwise objectionable brownish color imparted by the iodine.
The Pluronic F-68 which is a solid flake essentially of a predetermined molecular weight of the hydrophobic group and predetermined ratio of the hydrophylic group with respect thereto, is melted by heating to about 4'5 C., whereupon the iodine is dissolved by mixing therewith. Then the Carbowax in flake form is dissolved therewith, with additional heating if necessary. The resultant mass is then milled into the remaining components of the soap which is thereupon extruded in conventional manner to bar stock and cut into cakes.
The soap stock could be of any of numerous commercial types, preferably of low moisture content, such as the hard tallow type.
Example V.--Oral lozenges Such lozenge prepared with any of the usual components of sugar, water and flavoring matter may have incorporated therein 1.0 to 5.0%, preferably about 3.0% of Pluronic F-68 which has incorporated therein, in the manner set forth in Example IV, 0.1 to 0.5, preferably 0.2% iodine, with the efliective germicidal action noted and without impairing the taste or inducing any toxic effect.
Example VI.-Dry germicidal composition Parts Ureanitrate 70 to 90 preferably Pluronic F-68 10 to 20 preferably 15 Iodine 2 to 10 preferably 5 The iodine is dissolved in Pluronic F-68 in manner similar to that of example IV and the resultant liquid is added to the ureanitrate, the mixture being comminuted after it solidifies upon cooling.
In this solid composition, the halophor index of iodine with respect to the Pluronic may be exceeded somewhat without ensuing serious consequences following dilution in water. However, it is in general preferred to keep the iodine content within the halophor index.
The foregoing composition is a. free flowing dry powder and by reason of its large content of ureanitrate is of low cost.
While Pluronic F-68 is at present preferred, it is understood that other Pluronics which are solid at room temperature may be suitable for the purpose.
All of the compositions according to the present invention are readily soluble in any tap water to bring the Pluronic component with the free iodine therein into aqueous solution, without loss of iodine, but with ready and efiective release in the presence of microorganisms of only so much iodine as is required for effective and economical germicidal action. The composition is nontoxic orally and dermatologically and loses no iodine either by precipitation or vaporization.
As many changes could be made in the above composition and method and many apparently widely different embodiments of this invention could be made without departing from the scope of the claims, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.
Having thus described our invention, what we claim as new and desire to secure by Letters Patent of the United States is:
1. A germicidal composition comprising a nonionic carrier-iodine complex in the form of a solution of iodine with the nonionic carrier wherein a portion of the total iodine is chemically bound to said carrier and the major portion of the total iodine is loosely bound to said carrier and titratable asfree iodine, said carrier being a compound of the formula where y equals at least and (C2H40)a:+a: equals to 90% of the total weight of said compound, and the total iodine present in said complex being within a range having as a lower limit the amount to provide a germicidally effective quantity of loosely bound titratable iodine and as an upper limit about 28% by weight of said complex.
2. A germicidal composition as defined in claim 1, containing about 0.5 to 3% of an acid compatible with iodine and with said nonionic carrier.
3. A germicidal composition as defined in claim 1, containing about 0.5 to 3% of hydrochloric acid.
4. A germicidal composition as defined in claim 1 wherein the group (C3H60)y has a molecular weight within the range 1501 to 1800.
5. A germicidal composition as defined in claim 1, wherein the group (C3H60)y has a molecular weight within the range 1501 to 1800 and the groups comprise 20% to 30% by weight of the compound.
6. A germicidal composition as defined in claim 1, wherein the group (CsHeOh has a molecular weight within the range 1501 to 1800 and the groups comprise 40% to 50% by Weight of the compound.
7. A germicidal composition as defined in claim 1, wherein the group (C3H60)y has a molecular weight Within the range 1501 to 1800 and the groups comprise 80% to 90% by Weight of the compound.
8. A germicidal composition as defined in claim 1, containing in combination with said complex a lesser amount of a second complex of iodine with nonionic carrier, wherein the nonionic carrier is nonyl-phenol ethylene oxide condensate containing 8 to 9 mols of ethylene oxide per mol of nonyl-phenol.
9. A germicidal composition as defined in claim 8, wherein the carriers in said two complexes are present in proportions of about 5 to parts of the second named carrier to each 44 parts of the first named carrier.
10. A germicidal composition as defined in claim 1,
where y equals at least 15 and (C2H40):r+z;' equals 20 to 90% of the total weight of said carrier, that comprises mixing said carrier with an amount of elemental iodine to provide not more than about 28% iodine in the resulting complex in the presence of an acid which is inert to iodine, and agitating the mass while heating to a temperature of about 45 to C. until all the iodine is dissolved.
15. The method of preparing a complex of iodine and a nonionic carrier of the formula where y equals at least 15 and (c2H40):r+a:' equals 20 to of the total weight of said carrier with an amount of elemental iodine to provide not more than about 28% iodine in the resulting complex in the presence of hydrochloric acid, and agitating the mass while heating to a temperature of about 60 C. until all the iodine is dissolved.
References Cited in the file of this patent I UNITED STATES PATENTS 1,429,276 Davis Sept. 19, 1922 1,557,266 Moore Oct. 13, 1925 2,213,477 Steindorff et al. Sept. 3, 1940 2,275,979 Molnar Mar. 10, 1942 2,385,394 Witte Sept. 25, 1945 2,425,845 Toussaint et al. Aug. 19, 1947 2,550,622 Taub Apr. 24, 1951 2,599,140 Taub June 3, 1952 OTHER REFERENCES U. S. Dispensatory, 24th ed., 1947, Lippincott Co., Philadelphia, Pa., page 573.
Chemical Abstracts, vol. 44, 1950, page 11130a.
Chemical and Eng. News, February 19, 1951, vol. 29, page 664.
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|U.S. Classification||424/672, 510/389, 510/391, 510/514, 510/131, 514/772, 510/133, 510/421|
|International Classification||C11D1/00, A01N59/12|
|Cooperative Classification||C11D1/00, A01N59/12|
|European Classification||A01N59/12, C11D1/00|